Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,558 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,558 in last 12 months

Showing 1662116640 of 49,744 recalls

Medical DeviceDecember 11, 2020· Baxter Healthcare Corporation

Recalled Item: VERITAS Collagen Matrix - Product Usage: intended for use in Recalled by...

The Issue: VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide...

The Issue: VITROS Chemistry Products CKMB Slides Potential for Falsely Elevated Results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 10, 2020· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...

The Issue: Subpotent Drug: Low out-of-specification assay results for the epinephrine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 10, 2020· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 600FP Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...

The Issue: Due to a manufacturing error their is a potential that the sheath within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Remel Inc

Recalled Item: Remel Blood Agar/MacConkey Agar Bi-Plate Recalled by Remel Inc Due to The...

The Issue: The blood agar side of the bi-plate may not grow some patient isolates or QC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Clerio Vision

Recalled Item: Clerio Vision Recalled by Clerio Vision Due to One lot of contact lenses...

The Issue: One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Accuray Incorporated

Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...

The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Accuray Incorporated

Recalled Item: TomoTherapy Treatment System - Product Usage: used as an integrated Recalled...

The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 9, 2020· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...

The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Biogen MA Inc.

Recalled Item: Vumerity (diroximel fumarate) delayed-release capsule Recalled by Biogen MA...

The Issue: Failed dissolution specifications: out-of-specification test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Imatinib Mesylate Tablets 400 mg Recalled by Shilpa Medicare Limited Due to...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund